1. Homozygous Robertsonian translocations in a fetus with 44 chromosomes

   • C. Rockman-Greenberg
   • M. Ray
   • J. L. Hamerton

   Original Investigations 01 October 1982 Pages: 181 - 184

2. Diphenoloxidases in various forms of myopathy which are transmitted by different genetic mechanisms

   • Jean J. Demos
   • David G. Tuil
   • Pierre C. Katz

   Original Invesigations 01 October 1982 Pages: 185 - 189

3. Nondisjunction and chromosome breakage in mouse oocytes after various X-ray doses

   • I. Hansmann
   • J. Jenderny
   • H. D. Probeck

   Original Invesigations 01 October 1982 Pages: 190 - 192

4. Population genetical aspects of primary congenital glaucoma. I. Incidence, prevalence, gene frequency, and age of onset

   • A. Genčík
   • A. Genčíkova
   • V. Ferák

   Original Invesigations 01 October 1982 Pages: 193 - 197

5. Population genetic aspects of primary congenital glaucoma. II. Fitness, parental consanguinity, founder effect

   • V. Ferák
   • A. Genčík
   • A. Genčíkova

   Original Invesigations 01 October 1982 Pages: 198 - 200

6. Similar chromosomal abnormalities in several retinoblastomas

   • Lundmila E. Kusnetsova
   • Elena L. Prigogina
   • Bella M. Belkina

   Original Invesigations 01 October 1982 Pages: 201 - 204

7. Detection of carriers for duchenne muscular dystrophy. Quality control of creatine kinase assay

   • H. Plauchu
   • C. Junien
   • J. M. Lalouel

   Original Invesigations 01 October 1982 Pages: 205 - 209

8. Polymorphism of the haptoglobin peptides by isoelectric focusing electrophoresis and isoelectric point determinations

   • K. Shibata
   • J. Constans
   • H. Matsumoto

   Original Invesigations 01 October 1982 Pages: 210 - 214

9. Prenatal diagnosis and outcome of pregnancy in 2036 women investigated by amniocentesis

   • Jeremy A. Squire
   • Lesley Nauth
   • Carol Timberlake

   Original Invesigations 01 October 1982 Pages: 215 - 222

10. Analysis of the breakpoints in translocation (15;17) Observed in 4 patients with acute promyelocytic leukemia

    • A. Hagemeijer
    • B. Löwenberg
    • J. Abels

    Original Invesigations 01 October 1982 Pages: 223 - 227

11. Cytogenetic toxicity of antitumor platinum compounds in Fanconi's anemia

    • Everdina H. A. Poll
    • Fré Arwert
    • Aldur W. Eriksson

    Original Invesigations 01 October 1982 Pages: 228 - 230

12. Somatic cell hybridization studies on the genetic regulation and allelic mutations in metachromatic leukodystrophy

    • Patricia L. Chang
    • Nadia E. Rosa
    • Ronald G. Davidson

    Original Invesigations 01 October 1982 Pages: 231 - 235

13. The DNA tumor virus SV 40 induces gene mutations in human cells. Reversion of HPRT deficiency

    • Lieselotte Lübbe
    • Michael Strauss
    • Erhard Geissler

    Original Invesigations 01 October 1982 Pages: 236 - 241

14. Isoelectric focusing of human red cell phosphoglucomutase (PGM₁). Phenotype distribution in the population of Tuscany and two hereditary variants

    • M. Bargagna
    • L. Abbagnale

    Original Invesigations 01 October 1982 Pages: 242 - 245

15. Interphase flow-cytogenetics: Correlation of DNA fluorescence to aneuploidy in human fibroblast cultures

    • P. S. Rabinovitch
    • G. M. Martin
    • H. Hoehn

    Original Invesigations 01 October 1982 Pages: 246 - 249

16. The mode of inheritance of ovalocytosis/elliptocytosis in Malaysian Orang Asli families

    • Alan G. Fix
    • Adela S. Baer
    • L. E. Lie-Injo

    Original Invesigations 01 October 1982 Pages: 250 - 253

17. The expression of fragile X chromosomes in members of the same family at different times of examination

    • Gertrud Eberle
    • Merve Zankl
    • Heinrich Zankl

    Short Communications 01 October 1982 Pages: 254 - 255

18. A red cell pyruvate kinase mutant with normal L-type PK in the liver

    • Jeanne Etiemble
    • Christiane Picat
    • Pierre Boivin

    Short Communications 01 October 1982 Pages: 256 - 258

19. Lack of effect of vitamin C on the incidence of chromosome anomalies induced by influenza virus in germ cells of mice

    • Kalpagam Pichan
    • Hanumanlu Polasa

    Short Communications 01 October 1982 Pages: 259 - 261

20. Transmission of fragile (X)(q27) from normal male(s)

    • J. P. Fryns
    • H. Van Den Berghe

    Clinical Case Reports 01 October 1982 Pages: 262 - 263

21. Deletion of 13q in two patients with retinoblastoma, one probably due to 13q- mosaicism in the mother

    • Kyra Michalová
    • František Klouček
    • Jana Musilová

    Clinical Case Reports 01 October 1982 Pages: 264 - 266

22. Dentition of a 48,XYY,+21 male

    • Grant Townsend

    Clinical Case Reports 01 October 1982 Pages: 267 - 268

23. Lethal, neonatal, short-limbed platyspondylic dwarfism. A further variant?

    • R. M. Winter
    • E. M. Thompson

    Clinical Case Reports 01 October 1982 Pages: 269 - 272

24. A variant of the fra(X) syndrome

    • Erica M. Bühler
    • Faruk Hadziselimovic
    • Ulla Pira

    Clinical Case Reports 01 October 1982 Pages: 273 - 275

25. Interstitial deletion 46,XY,del(1)(q23q25)

    • A. O. Martin
    • J. Leigh Simpson

    Cases Observed 01 October 1982 Pages: 277 - 277

26. A new case of satellited Yq chromosome

    • M. J. Martín
    • T. Rodriguez
    • J. A. Abrisqueta

    Cases Observed 01 October 1982 Pages: 277 - 277

27. Announcements

    Announcement 01 October 1982 Pages: 279 - 279